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DISP1 (dispatched RND transporter family member 1)

Identity

Alias_namesdispatched homolog 1 (Drosophila)
Alias_symbol (synonym)DISPA
MGC13130
DKFZP434I0428
MGC16796
Other alias
HGNC (Hugo) DISP1
LocusID (NCBI) 84976
Atlas_Id 53490
Location 1q41  [Link to chromosome band 1q41]
Location_base_pair Starts at 222988431 and ends at 223179337 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
BCAS3 (17q23.2) / DISP1 (1q41)PPP1R15B (1q32.1) / DISP1 (1q41)BCAS3 17q23.2 / DISP1 1q41

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)DISP1   19711
Cards
Entrez_Gene (NCBI)DISP1  84976  dispatched RND transporter family member 1
AliasesDISPA
GeneCards (Weizmann)DISP1
Ensembl hg19 (Hinxton)ENSG00000154309 [Gene_View]  chr1:222988431-223179337 [Contig_View]  DISP1 [Vega]
Ensembl hg38 (Hinxton)ENSG00000154309 [Gene_View]  chr1:222988431-223179337 [Contig_View]  DISP1 [Vega]
ICGC DataPortalENSG00000154309
TCGA cBioPortalDISP1
AceView (NCBI)DISP1
Genatlas (Paris)DISP1
WikiGenes84976
SOURCE (Princeton)DISP1
Genetics Home Reference (NIH)DISP1
Genomic and cartography
GoldenPath hg19 (UCSC)DISP1  -     chr1:222988431-223179337 +  1q41   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)DISP1  -     1q41   [Description]    (hg38-Dec_2013)
EnsemblDISP1 - 1q41 [CytoView hg19]  DISP1 - 1q41 [CytoView hg38]
Mapping of homologs : NCBIDISP1 [Mapview hg19]  DISP1 [Mapview hg38]
OMIM607502   
Gene and transcription
Genbank (Entrez)AK023679 AK026114 AK056569 AK098669 AK125728
RefSeq transcript (Entrez)NM_032890
RefSeq genomic (Entrez)NC_000001 NC_018912 NG_009243 NT_004487 NW_004929294
Consensus coding sequences : CCDS (NCBI)DISP1
Cluster EST : UnigeneHs.692324 [ NCBI ]
CGAP (NCI)Hs.692324
Alternative Splicing GalleryENSG00000154309
Gene ExpressionDISP1 [ NCBI-GEO ]   DISP1 [ EBI - ARRAY_EXPRESS ]   DISP1 [ SEEK ]   DISP1 [ MEM ]
Gene Expression Viewer (FireBrowse)DISP1 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)84976
GTEX Portal (Tissue expression)DISP1
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96F81   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96F81  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96F81
Splice isoforms : SwissVarQ96F81
PhosPhoSitePlusQ96F81
Domaine pattern : Prosite (Expaxy)SSD (PS50156)   
Domains : Interpro (EBI)Patched    SSD   
Domain families : Pfam (Sanger)Patched (PF02460)   
Domain families : Pfam (NCBI)pfam02460   
Conserved Domain (NCBI)DISP1
DMDM Disease mutations84976
Blocks (Seattle)DISP1
SuperfamilyQ96F81
Human Protein AtlasENSG00000154309
Peptide AtlasQ96F81
HPRD06326
IPIIPI00172479   IPI00645249   
Protein Interaction databases
DIP (DOE-UCLA)Q96F81
IntAct (EBI)Q96F81
FunCoupENSG00000154309
BioGRIDDISP1
STRING (EMBL)DISP1
ZODIACDISP1
Ontologies - Pathways
QuickGOQ96F81
Ontology : AmiGOprotein binding  smoothened signaling pathway  smoothened signaling pathway  patched ligand maturation  determination of left/right symmetry  hedgehog receptor activity  embryonic pattern specification  dorsal/ventral pattern formation  peptide transporter activity  peptide transport  integral component of membrane  diaphragm development  
Ontology : EGO-EBIprotein binding  smoothened signaling pathway  smoothened signaling pathway  patched ligand maturation  determination of left/right symmetry  hedgehog receptor activity  embryonic pattern specification  dorsal/ventral pattern formation  peptide transporter activity  peptide transport  integral component of membrane  diaphragm development  
NDEx NetworkDISP1
Atlas of Cancer Signalling NetworkDISP1
Wikipedia pathwaysDISP1
Orthology - Evolution
OrthoDB84976
GeneTree (enSembl)ENSG00000154309
Phylogenetic Trees/Animal Genes : TreeFamDISP1
HOVERGENQ96F81
HOGENOMQ96F81
Homologs : HomoloGeneDISP1
Homology/Alignments : Family Browser (UCSC)DISP1
Gene fusions - Rearrangements
Fusion : MitelmanBCAS3/DISP1 [17q23.2/1q41]  [t(1;17)(q41;q23)]  
Fusion: TCGABCAS3 17q23.2 DISP1 1q41 BRCA
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerDISP1 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)DISP1
dbVarDISP1
ClinVarDISP1
1000_GenomesDISP1 
Exome Variant ServerDISP1
ExAC (Exome Aggregation Consortium)DISP1 (select the gene name)
Genetic variants : HAPMAP84976
Genomic Variants (DGV)DISP1 [DGVbeta]
DECIPHER (Syndromes)1:222988431-223179337  ENSG00000154309
CONAN: Copy Number AnalysisDISP1 
Mutations
ICGC Data PortalDISP1 
TCGA Data PortalDISP1 
Broad Tumor PortalDISP1
OASIS PortalDISP1 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICDISP1  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDDISP1
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch DISP1
DgiDB (Drug Gene Interaction Database)DISP1
DoCM (Curated mutations)DISP1 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)DISP1 (select a term)
intoGenDISP1
Cancer3DDISP1(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM607502   
Orphanet20436    20435    18904    12486    12484    12485   
MedgenDISP1
Genetic Testing Registry DISP1
NextProtQ96F81 [Medical]
TSGene84976
GENETestsDISP1
Huge Navigator DISP1 [HugePedia]
snp3D : Map Gene to Disease84976
BioCentury BCIQDISP1
ClinGenDISP1 (curated)
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD84976
Chemical/Pharm GKB GenePA134938043
Clinical trialDISP1
Miscellaneous
canSAR (ICR)DISP1 (select the gene name)
Probes
Litterature
PubMed13 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineDISP1
EVEXDISP1
GoPubMedDISP1
iHOPDISP1
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 13:03:20 CET 2017

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